Benzyl pent-4-ynoate

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Reagent Code: #83861
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CAS Number 126378-11-8

science Other reagents with same CAS 126378-11-8

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Weight 188.22 g/mol
Formula C₁₂H₁₂O₂
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MDL Number MFCD22023868
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Benzyl pent-4-ynoate is widely used in organic synthesis as a versatile building block, particularly in the creation of complex molecules. Its alkyne functional group makes it valuable in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is essential for developing pharmaceuticals, bioconjugates, and polymers. Additionally, it serves as an intermediate in the synthesis of bioactive compounds, including potential drug candidates. Its benzyl ester group also allows for selective deprotection, making it useful in multi-step synthetic processes. This compound is particularly favored in medicinal chemistry for designing molecules with targeted biological activities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,564.00
inventory 250mg
10-20 days ฿6,390.00
inventory 1g
10-20 days ฿12,780.00

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Benzyl pent-4-ynoate
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Benzyl pent-4-ynoate is widely used in organic synthesis as a versatile building block, particularly in the creation of complex molecules. Its alkyne functional group makes it valuable in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is essential for developing pharmaceuticals, bioconjugates, and polymers. Additionally, it serves as an intermediate in the synthesis of bioactive compounds, including potential drug candidates. Its benzyl ester group also

Benzyl pent-4-ynoate is widely used in organic synthesis as a versatile building block, particularly in the creation of complex molecules. Its alkyne functional group makes it valuable in click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), which is essential for developing pharmaceuticals, bioconjugates, and polymers. Additionally, it serves as an intermediate in the synthesis of bioactive compounds, including potential drug candidates. Its benzyl ester group also allows for selective deprotection, making it useful in multi-step synthetic processes. This compound is particularly favored in medicinal chemistry for designing molecules with targeted biological activities.

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